Involvement of Vitamin D Receptor Gene Polymorphism in Increased Cardiovascular Risk Disease in the Algerian
Assia Galleze1, Fatma Zohra Djaballah-Ider1, Ines Gouaref2
1Department of Cellular and Molecular Biology, Faculty of Biological Sciences, Houari Boumediene University of Sciences and Technology, Algiers 16111, Algeria.
Insights
Vitamin D receptor (VDR) gene variations, specifically the ApaI polymorphism, are linked to cardiovascular diseases (CVDs) and heart failure (HF) risk in Algeria. Lower vitamin D levels correlate with increased cardiovascular risk.
Area of Science:
- Genetics
- Endocrinology
- Cardiology
Background:
- Cardiovascular diseases (CVDs), including heart failure (HF), represent a significant global health burden.
- Vitamin D plays a crucial role in cardiovascular system regulation.
- The vitamin D receptor (VDR) gene is a potential factor in CVD development.
Purpose of the Study:
- To investigate the association between VDR gene polymorphisms and cardiovascular disorders in the Algerian population.
- To explore the relationship between VDR genotypes, vitamin D levels, and NT-proBNP in CVD patients.
Main Methods:
- VDR gene polymorphisms (ApaI) identified using PCR-RFLP.
- Plasma 25-hydroxyvitamin-D levels measured by chemiluminescent immunoassay.
- Plasma NT-proBNP levels determined by immunoenzymatic analysis.
Main Results:
- ApaI VDR gene polymorphism frequencies were significantly higher in CVD patients versus controls.
- Higher prevalence of AA genotypes and A alleles observed in the CVD group.
- CVD patients with HF showed similar genotype/allele distributions compared to those without HF.
- Lower vitamin D levels and higher NT-proBNP levels were associated with VDR rs7975232 genotype in CVD patients.
Conclusions:
- ApaI polymorphism of the VDR gene and low vitamin D levels may increase cardiovascular risk.
- The VDR ApaI AA genotype could serve as a novel risk marker for heart failure in the Algerian population.
Abstract:
Cardiovascular diseases (CVDs) cover various pathologies including heart failure (HF). Furthermore, vitamin D is involved in the regulation of the cardiovascular system. This study aimed to assess the association between the vitamin D receptor (VDR) genotypes and the occurrence of cardiovascular disorders in the Algerian population. VDR gene polymorphisms were identified using the PCR-RFLP method. Moreover, plasma concentrations of 25-hydroxyvitamin-D were assessed by a chemiluminescent immunoassay method and plasma NT-proBNP levels were determined in vitro by immunoenzymatic analysis. Interestingly, our results indicate that the genotypic frequencies of ApaI polymorphism of the VDR gene were significantly higher in CVD patients compared to the control group. Moreover, higher numbers of AA genotypes and A alleles were found in the CVD group. Our data indicate that the group of CVD patients with HF compared to those without HF showed the same genotype and allele distribution. Furthermore, low vitamin D rates and high N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels according to the VDR rs7975232 genotype were noted in CVD patients compared to healthy controls. Our results indicate that ApaI polymorphism of the VDR gene and lower vitamin D level may be associated with increased cardiovascular risk. These findings indicate that the ApaI AA genotype could be considered as a new HF risk marker in the Algerian population.
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